Soft tissue sarcoma incidences and clinical characteristics are significantly different in France and Taiwan.


Journal

Cancer
ISSN: 1097-0142
Titre abrégé: Cancer
Pays: United States
ID NLM: 0374236

Informations de publication

Date de publication:
15 09 2022
Historique:
revised: 23 05 2022
received: 09 01 2022
accepted: 27 05 2022
pubmed: 8 7 2022
medline: 31 8 2022
entrez: 7 7 2022
Statut: ppublish

Résumé

The incidence of different soft tissue sarcoma (STS) histotypes among ethnic and geographic populations has not been comprehensively investigated. Data from 2013 to 2016 were obtained from national cancer registry databases in France and Taiwan. Liposarcoma (LPS), leiomyosarcoma (LMS), angiosarcoma (AS), synovial sarcoma (SS), and malignant peripheral nerve sheath tumor (MPNST) were selected as index STSs to estimate the age-standardized incidence rates (ASRs) and other clinical features between patients. In total, 9398 patients (7148 from France and 2250 from Taiwan) were included. The ASRs of AS (5.4 vs. 2.8) and MPNST (2.0 vs. 1.0) were significantly higher in Taiwan; France had significantly higher ASRs for LPS (12.0 vs. 10.0), LMS (9.7 vs. 7.6), and SS (1.7 vs. 1.2). Patients in Taiwan with LMS or LPS were younger than their French counterparts. With regard to the distribution according to primary anatomic site, French patients had higher odds for extremity and truncal LMS (odds ratio [OR], 2.84; p < .001), AS (OR, 2.67; p < .001), MPNST (OR, 1.55; p = .027), and LPS (OR, 1.38; p < .001) and for breast AS (OR, 10.58; p < .001). Taiwanese patients had higher odds for liver AS (OR, 10.72; p < .001) and uterine LMS (OR, 3.21; p < .001). SS age and distribution according to primary anatomic site did not differ significantly between the French and Taiwanese populations. Significant differences in the incidence and clinical characteristics of index STS suggested that geographic (environmental) and ethnicity factors likely play a vital role in the pathogenesis of STS.

Sections du résumé

BACKGROUND
The incidence of different soft tissue sarcoma (STS) histotypes among ethnic and geographic populations has not been comprehensively investigated.
METHODS
Data from 2013 to 2016 were obtained from national cancer registry databases in France and Taiwan. Liposarcoma (LPS), leiomyosarcoma (LMS), angiosarcoma (AS), synovial sarcoma (SS), and malignant peripheral nerve sheath tumor (MPNST) were selected as index STSs to estimate the age-standardized incidence rates (ASRs) and other clinical features between patients.
RESULTS
In total, 9398 patients (7148 from France and 2250 from Taiwan) were included. The ASRs of AS (5.4 vs. 2.8) and MPNST (2.0 vs. 1.0) were significantly higher in Taiwan; France had significantly higher ASRs for LPS (12.0 vs. 10.0), LMS (9.7 vs. 7.6), and SS (1.7 vs. 1.2). Patients in Taiwan with LMS or LPS were younger than their French counterparts. With regard to the distribution according to primary anatomic site, French patients had higher odds for extremity and truncal LMS (odds ratio [OR], 2.84; p < .001), AS (OR, 2.67; p < .001), MPNST (OR, 1.55; p = .027), and LPS (OR, 1.38; p < .001) and for breast AS (OR, 10.58; p < .001). Taiwanese patients had higher odds for liver AS (OR, 10.72; p < .001) and uterine LMS (OR, 3.21; p < .001). SS age and distribution according to primary anatomic site did not differ significantly between the French and Taiwanese populations.
CONCLUSIONS
Significant differences in the incidence and clinical characteristics of index STS suggested that geographic (environmental) and ethnicity factors likely play a vital role in the pathogenesis of STS.

Identifiants

pubmed: 35796499
doi: 10.1002/cncr.34372
doi:

Substances chimiques

Lipopolysaccharides 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3360-3369

Informations de copyright

© 2022 American Cancer Society.

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Auteurs

Tom Wei-Wu Chen (TW)

Department of Oncology, National Taiwan University Hospital, Taipei, Taiwan.
Graduate Institute of Oncology, National Taiwan University College of Medicine, Taipei, Taiwan.

Ruru Chun-Ju Chiang (RC)

Institute of Epidemiology and Preventive Medicine, College of Public Health, National Taiwan University, Taipei, Taiwan.
Taiwan Cancer Registry, Taipei, Taiwan.

Alex Le Cesne (A)

Medical Oncology, Gustave Roussy Institute-Cancer Campus, Villejuif, France.

Yu-Chun Hsieh (YC)

Health Data Research Center, National Taiwan University, Taipei, Taiwan.

Antoine Italiano (A)

Early Phase Trials Unit, Bergonie Institute, Bordeaux, France.

Ya-Wen Yang (YW)

Institute of Epidemiology and Preventive Medicine, College of Public Health, National Taiwan University, Taipei, Taiwan.
Taiwan Cancer Registry, Taipei, Taiwan.

Nicolas Penel (N)

General Oncology Department, Oscar Lambret Center, Lille, France.

Wen-Chung Lee (WC)

Institute of Epidemiology and Preventive Medicine, College of Public Health, National Taiwan University, Taipei, Taiwan.
Taiwan Cancer Registry, Taipei, Taiwan.

Emmanuelle Bompas (E)

Western Oncology Institute, Nantes, France.

Thibaud Valentin (T)

Claudius Regaud Institute, Toulouse, France.

Philippe Anract (P)

Department of Orthopedics, Assistance publique Hopitaux de Paris, Paris, France.

Nelly Firmin (N)

Montpellier Cancer Institute, Montpellier, France.

Florence Duffaud (F)

Medical Oncology, Greater Paris University Hospitals, Marseilles, France.

Ann-Lii Cheng (AL)

Department of Oncology, National Taiwan University Hospital, Taipei, Taiwan.
Graduate Institute of Oncology, National Taiwan University College of Medicine, Taipei, Taiwan.

Francoise Ducimetiere (F)

Medicine Department, Leon Berard Center, Lyon, France.

K Arnold Chan (KA)

Graduate Institute of Oncology, National Taiwan University College of Medicine, Taipei, Taiwan.

Jean-Yves Blay (JY)

Medicine Department, Leon Berard Center, Lyon, France.

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